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  • 121 Request Info

    Webinar on Cal/OSHA Update for 2019: Impact on California Employers

    Gain insight on recent and upcoming Cal/OSHA regulatory developments and trends that will impact California employers in 2019-which is right around the corner. Price:$200.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 info@onlinecompliancepanel.com Event link - https://www.onlinecompliancepanel.com/webinar/Cal-OSHA-Update-for-2019-Hot-Spots-Practical-Compliance-Strategies-Every-Safety-Pro-Should-Know-505987/APRIL-2019-ES-TRAININGREGISTRY
  • 122 Request Info

    Webinar on CAMELS Evaluation and Ratings System plus Examination of CCAR and CLAR

    The webinar will provide an in depth understanding of the CAMELS methodology and evaluation process in order to address any deficiencies that may exist before a CAMELS evaluation is conducted. Attendees will gain an in depth understanding of the FRB's approach to its CCAR and CLAR evaluation considerations, processes and ratings. Price:$200.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 info@onlinecompliancepanel.com Event link https://www.onlinecompliancepanel.com/webinar/CAMELS-Evaluation-and-Ratings-System-plus-Examination-of-CCAR-and-CLAR-503046/MARCH-2018-ES-TRAININGREGISTRY
  • 123 Request Info

    Webinar on CAPA Simplified - A One-Form, Easy-To-Complete, Method for Simplifying Your CAPA Process

    Learn 21 CFR subpart J of FDA regulations related to CAPA, how to integrate CAPA with other branches of QMS. Price:$200.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 info@onlinecompliancepanel.com Event link https://www.onlinecompliancepanel.com/webinar/CAPA-Simplified-A-One-Form-Easy-To-Complete-Method-for-Simplifying-Your-CAPA-Process-507402/JULY-2018-ES-TRAININGREGISTRY
  • 124 Request Info

    Webinar on Capital Equipment Procurement

    With everyone working very hard to make money, it is surprising how many organizations allow much of this money to be wasted by poor purchasing practices in obtaining capital equipment. This webinar is designed to stop the waste by providing some of the principles and concepts of best procurement practices to all those involved in the specifying, selection and contracting for capital equipment. Price:$200.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 info@onlinecompliancepanel.com Event link https://www.onlinecompliancepanel.com/webinar/Capital-Equipment-Procurement-505232/JANUARY-2018-ES-TRAININGREGISTRY
  • 125 Request Info

    Webinar On Capturing Justifications in Change Control, Risk Assessment, Validations, and Investigations

    In this webinar, you will learn about analyses which are regarded as compliant and convenient ways to justify and confirm projects such as Change Controls, Risk Assessments, Validations and Investigations.Price:$250.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 info@onlinecompliancepanel.com Event link http://www.onlinecompliancepanel.com/webinar/CAPTURING-JUSTIFICATIONS-501953/FEBRUARY-2017-ES-TRAININGREGISTRY
  • 126 Request Info

    Webinar On CE Mark - Required to Sell in the European Market

    Medical devices sold into the European Union (EU) must comply with the applicable medical device directives, EU laws similar to FDA's regulations. Medical devices declared compliant must bear a CE mark in order to be admitted into the 29 member countries comprising the EU.Price:$250.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 info@onlinecompliancepanel.com Event link http://onlinecompliancepanel.com/webinar/CE-MARK-REQUIRED-SELL-EUROPEAN-MARKET-501636/AUGUST-2016-ES-TRAININGREGISTRY
  • 127 Request Info

    Webinar On Cleaning Validations Using Extraction Techniques

    Cleaning validations are an essential step in the medical device development process. One of the most common methods is using extraction techniques to validate the cleanliness of a device. This webinar will provide valuable guidance on how to achieve a thorough validation of a cleaning process. These cleaning processes may include initial cleaning validations, in process cleaning validations, or reprocess cleaning validations.Price:$250.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 info@onlinecompliancepanel.com Event link http://www.onlinecompliancepanel.com/webinar/CLEANING-VALIDATIONS-EXTRACTION-TECHNIQUES-503258/JUNE-2017-ES-TRAININGREGISTRY
  • 128 Request Info

    Webinar on Cleaning Validations Using Extraction Techniques

    This webinar will provide valuable guidance on how to use extraction techniques to validate the cleanliness of a device. Price:$200.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 info@onlinecompliancepanel.com Event link - https://www.onlinecompliancepanel.com/webinar/Cleaning-Validations-Using-Extraction-Techniques-504912/MARCH-2019-ES-TRAININGREGISTRY
  • 129 Request Info

    Webinar On Clinical System Data Management Validation

    Have you validated your clinical data base? Do you have the proper documentation in the event of a regulatory inspection? In this course we will cover considerations and requirements for validation of clinical data management systems. We will discuss the challenges and strategies of risk based validation and review 21 CFR Part 11 expectations. We will discuss the importance of a change control process.Price:$250.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 info@onlinecompliancepanel.com Event link http://onlinecompliancepanel.com/webinar/CLINICAL-DATA-MANAGEMENET-501926/DECEMBER-2016-ES-TRAININGREGISTRY
  • 130 Request Info

    Webinar on CMC Requirements for Cell and Gene Therapy

    Learn how your company can keep its best and brightest future leaders by applying the best practice strategies provided by Wes Pruett in this training. Price:$200.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 info@onlinecompliancepanel.com Event link https://www.onlinecompliancepanel.com/webinar/CMC-Requirements-for-Cell-and-Gene-Therapy-508889/APRIL-2018-ES-TRAININGREGISTRY
  • 131 Request Info

    Webinar on Common Problems and Mistakes in Method Validation in Drug Development Process

    This webinar provides information that will identify and correct common issues that may arise during validation of methods required in drug development. Price:$250.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 info@onlinecompliancepanel.com Event link https://www.onlinecompliancepanel.com/webinar/Common-Problems-and-Mistakes-in-Method-Validation-in-Drug-Development-Process-505094/JULY-2018-ES-TRAININGREGISTRY
  • 132 Request Info

    Webinar On Comparability Protocols for Approved Drugs

    This webinar will address approaches to developing comparability protocols for approved drugs, including primary content considerations and timing of submission. The information obtained will enable completion of appropriate testing to make changes to the drug substance or drug product formulation, manufacturing facility, and container closure. The webinar will address aspects of preparing the protocol prior to confirmed changes in order to speed approval and preparing the appropriate updates to Module 3 of the CTD.Price:$250.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 info@onlinecompliancepanel.com Event link http://onlinecompliancepanel.com/webinar/COMPARABILITY-PROTOCOLS-APPROVED-DRUGS-501539/JUNE-2016-ES-TRAININGREGISTRY
  • 133 Request Info

    Webinar On Complaint Management: Complaint Handling in Compliance with FDA and ISO Regulations

    Complaint handling is likely one of the more cross-functional parts of your quality system: Customer Service may receive your customer complaints, Sales and Marketing may need to reach out to the customer for additional information, Regulatory Affairs may determine whether the complaint is reportable, QA may perform the root cause investigation, R&D or Manufacturing Engineering may need to be involved in the corrective action, and Quality Engineering may need to trend the complaints!Price:$250.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 info@onlinecompliancepanel.com Event link https://www.onlinecompliancepanel.com/webinar/COMPLAINT-MANAGEMENT-502650/AUGUST-2017-ES-TRAININGREGISTRY
  • 134 Request Info

    Webinar On Complaints, Servicing and FDA Reporting

    This presentation provides a framework for understanding, managing, and reporting adverse events to the FDA. It uses plain English to describe the regulatory requirements as well as common quality tools such as flow diagrams and fault tree analysis. This approach helps participants understand and implement the essential parts of the regulations.Price:$250.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 info@onlinecompliancepanel.com Event link http://onlinecompliancepanel.com/webinar/COMPLAINTS-SERVICING-FDA-REPORTING-507863/JUNE-2017-ES-TRAININGREGISTRY
  • 135 Request Info

    Webinar on Compliance Measures for Case Managers

    By attending this session you will be able to ensure that you understand the compliance issues directly related to the practice of case management and that you have incorporated them into your daily practice. Compliance includes documentation and communication with the patient and family as well. Be sure that your processes are hard-wired and part of your daily routine.Price:$200.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 info@onlinecompliancepanel.com Event link https://www.onlinecompliancepanel.com/webinar/Compliance-Measures-for-Case-Managers-508519/SEPTEMBER-2018-ES-TRAININGREGISTRY
  • 136 Request Info

    Webinar on Compliance Readiness: Being Prepared for a Software License Audit

    In this webinar, you will understand the different approaches to achieve contract compliance in the area of Software Licence Management. A software license audit can cause severe disruption and takes time and resources away from business as usual.Price:$200.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 info@onlinecompliancepanel.com Event link https://www.onlinecompliancepanel.com/webinar/Compliance-Readiness-Being-Prepared-for-a-Software-License-Audit-509355/SEPTEMBER-2018-ES-TRAININGREGISTRY
  • 137 Request Info

    Webinar On Compliance with ICH GCP R2 Addendum for Auditors

    This New ICH GCP E6 Revision 2 changes will cover those new requirements for running clinical trials, evaluate the changes and discuss how to implement these for sponsors, CROs and study sites. This session will enable you to meet the new international GCP standard to ensure the acceptance of clinical trial data by the regulatory authorities internationally including the European Union (EU), Japan, the United States, Canada and Switzerland.Price:$200.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 info@onlinecompliancepanel.com Event link http://www.onlinecompliancepanel.com/webinar/COMPLIANCE-ICH-GCP-R2-ADDENDUM-AUDITORS-505313/JUNE-2017-ES-TRAININGREGISTRY
  • 138 Request Info

    Webinar on Comply US Customs Importing Requirements and the MOD Act

    Attend this introductory trade logistic session that provide valuable assistance to corporate import team and give company the tools to assess potential gaps. Price:$200.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 info@onlinecompliancepanel.com Event link https://www.onlinecompliancepanel.com/webinar/Complying-with-Customs-laws-and-Responsibilities-under-the-Customs-Modernization-Act-507252/AUGUST-2018-ES-TRAININGREGISTRY
  • 139 Request Info

    Webinar on Complying with FDA's Regulations for eCTD Submissions of all IND's NDA's

    How to ensure that you are ready for implementing the mandated requirements of the CTD & eCTD how to comply with the May 2018 electronic submission requirements Price:$350.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 info@onlinecompliancepanel.com Event link https://www.onlinecompliancepanel.com/webinar/Complying-with-FDA-s-Regulations-for-eCTD-Submissions-of-all-IND-s-NDA-s-Are-you-Ready-for-the-May-5-2018-deadline-506512/APRIL-2018-ES-TRAININGREGISTRY
  • 140 Request Info

    Webinar On Conducting a Software Validation of Medical Device to Meet FDA Requirements

    This course will teach how to conduct a software validation program that will satisfy FDA requirements and produce a safe product. We will explain the role of risk analysis in validation. How software requirements are used in validation will be described. This course is not a programming course. We will discuss what must be done but will not discuss methods to execute necessary testing.Price:$250.00. Contact info : OnlineCompliancePanel Phn. no. +1-510-857-5896 Fax-+1-510-509-9659 info@onlinecompliancepanel.com Event link http://onlinecompliancepanel.com/webinar/SOFTWARE-VALIDATION-MEDICAL-DEVICE-501884/NOVEMBER-2016-ES-TRAININGREGISTRY